Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 3-Methoxybenzyl bromide | HCID 4067207 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Bromo-5-methoxybenzyl bromide | HCID 3525951 | 72.1% |
Reaction Steps
To a solution of above-described crude 1-(bromomethyl)-3-methoxybenzene (152.5 g) in 1 L of chloroform a solution of 134 g (0.841 mol) of bromine in 200 ml of chloroform was added dropwise by vigorous stirring at room temperature. The reaction mixture was stirred overnight at ambient temperature and then evaporated to dryness. The residue was triturated with 1000 ml of n-hexane, and the precipitate was filtered off, washed with 100 ml of n-hexane, and then dried in vacuum. An additional amount of the product was obtained by evaporation of mother liquor followed by treatment of the residue with 200 ml of n-hexane. In total, this procedure gave 153 g (55% overall yield for two stages) of 1-bromo-2-(bromomethyl)-4-methoxybenzene. (average of two runs)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187583B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-06529ac9ae0a4d9cb5293fee4379941e |
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| Source note | uspto-grants-2015_11 |
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